Clinical Pediatric Endocrinology
Online ISSN : 1347-7358
Print ISSN : 0918-5739
ISSN-L : 0918-5739
Mutation-in-Brief
H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
Keisuke NagasakiTakeshi UsuiTadashi AsamiYohei OgawaToru KikuchiMakoto Uchiyama
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2009 Volume 18 Issue 4 Pages 111-113

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© 2009 by The Japanese Society for Pediatric Endocrinology
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